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Care Act Expert Webinar
Providing Good Information,
Advice and Advocacy
1
Webinar aims
We will explore
• The changes to the law regarding information,
advice and advocacy and how these fit with the
wider aims of the Care Act
• The related challenges, and some examples of how
these are being addressed in different areas
2
Webinar objectives
By the end of this webinar, you will have
• Begun to consider how effectively your existing
services meet the requirements of the Care Act
• Identified barriers and enablers to meeting these
requirements
• Examined key examples of good practice
• Started to identify next steps in your area
3
Webinar agenda
1. Definitions
2. What’s working at the moment?
3. The changes to the law
4. Getting your own information across
5. Coordinating provision of information and advice
6. Independent advocacy – why it matters
7. Final thoughts
4
Definitions
5
Definitions from the Care Act Guidance
Information means the communication of
knowledge and facts regarding care and support.
It can be subdivided into ‘self-help’ and ‘assisted’
information
Advice means helping a person to identify choices
and/or providing an opinion or recommendation
regarding a course of action in relation to care
and support.
6
Definitions from the Care Act Guidance
Financial information and advice covers services
whose purpose is to help people plan, prepare and
pay for their care costs. ‘Independent’ financial
information or advice means services independent
of the local authority.
Advocacy means supporting a person to understand
information, express their needs and wishes,
secure their rights, represent their interests and
obtain the care and support they need.
7
A degree of overlap
8
e.g.
leaflet;
website
e.g.
helpline,
library
e.g.
social
worker, GP
e.g.
financial
advisor
e.g.
advocate,
family
member
Self-help
information
Assisted
information
Advice
Specialist
advice
Advocacy
What’s working at the moment?
What challenges are you facing in the provision of
information, advice and advocacy?
In which areas are you well prepared and on track?
9
Changes to the law
10
The wider context of the Care Act
• Long overdue bringing together of the patchwork
of adult social care legislation
• Changing relationship between people and services
• A move from dependency to empowerment –
assisting people and communities to find
sustainable solutions
• Dwindling resources and increased demand 11
Empowerment
Two senses:
1. Giving power (whether political, social or
economic) to someone
• This is what underlies notions of co-production
Or
2. Supporting someone to claim personal power.
• This is what underlies person-centred care and
an outcomes-based approach.
12
How does the Care Act empower?
1. Universal access to information and
advice
1. Informing people so they can make the best
choices for themselves: starting from the notion
that people are experts in what’s best for them
2. This responsibility extends to all citizens, not just
those with eligible needs
3. This links to the council’s preventative role: it
empowers people by helping to keep their options
open; by preventing/delaying/reducing needs for
care and support.
13
How does the Care Act empower?
2. Improved access to advocacy
1. Although far from universal (as we’ll see below),
the role of independent advocacy is a recognition
of the power of advocacy
2. LAs have the option of providing advocacy more
widely than the Care Act requires. Rather than
simply a communication aid, advocacy can be
seen as protector of the person’s human rights.
14
The prevention agenda
The provision of information, advice and advocacy is
part of addressing the aim of preventing, delaying
and reducing people’s need for care and support:
• With good information and advice, people can
make better, healthier decisions
• It is important for tackling the issue of multiple
needs and exclusions
• help to access specialist support or common
interest groups
• advocacy promotes the individual’s rights and
interests and hence their wellbeing 15
The letter of the law:
information and advice
Section 4 of the Care Act specifies that an LA must
‘establish and maintain a service for providing people
in its area with information and advice relating to
care and support for adults and support for carers’
including
• Types of care and support available and how to
access it
• How to access independent financial advice
• How to raise concerns
16
The letter of the law:
information and advice
The LA must also
• ensure information and advice provided is
accessible and proportionate
• ‘have regard to the importance of identifying those
individuals’ who would benefit from financial
advice
• Make sure that this advice is good enough to allow
them to plan and make decisions about their own
care.
17
Information and advice: what does
the Guidance say?
It is the LA’s responsibility to ensure the
• COHERENCE
• SUFFICIENCY
• AVAILABILITY
• ACCESSIBILITY
of information and advice relating to care and
support across its area (p23)
18
As well as covering basic information about what care and
support is available, this service needs to cover
• prevention of care and support needs
• finances
• health
• housing
• employment
• what to do in cases of abuse or neglect of an adult and other
areas where required (p23-24)
19
Information and advice: what does
the Guidance say?
This duty is about
• engaging with and understanding the needs of
people in your area and
• ensuring that the requirement to provide
information is met in the most appropriate way –
whether by the authority or another organisation.
• It falls on the authority to ‘understand, co-ordinate
and make effective use of’ other I&A resources in
your area
20
Information and advice: what does
the Guidance say?
The particular needs of carers may include:
• breaks from caring;
• the health and wellbeing of carers themselves;
• caring and advice on wider family relationships;
• carers’ financial and legal issues;
• caring and employment;
• caring and education; and,
• a carer’s need for advocacy.
21
Information and advice: what does
the Guidance say?
Getting your own information
across
22
Skills for Care resources
23
skillsforcare.org.uk
Provides slide
packs,
summaries, a
workbook
and case
studies.
Can be used
as the basis
for staff
development.
The RiPfA Practice
Tool
24
ripfa.org.uk
• Outlines good practice
regarding information
provision for different
groups
• Helps you audit the
information you provide
• Helps you ask service
users and carers what is
working and not working
• Tool to support reflection
Challenges in the provision of
information
• Generally people do not have a good
understanding of adult social care and there may
be stigma in approaching it (ADASS, 2011).
• Often people first seek information at a time of
crisis (Bottery and Holloway, 2013).
• Uncoordinated services will result in
uncoordinated, unreliable information (Anderson,
2011)
25
Challenges in the provision of
information
• Older people are less likely to use the internet or call centres
(Horton, 2009)
• BME groups face cultural and linguistic barriers (Zahno and
Rhule, 2008). An equality impact assessment on the
provision of information can address this (c.f. Newham’s
safeguarding work – see RiPfA blog 13/3/14)
• Self-funders may not be seen as a priority (Hudson and
Henwood, 2009)
• Many people face difficulties with communication or capacity
(IDEA, 2009)
• People who face stigma are less likely to engage with social
care (RiPfA, 2013).
26
Good practice in the provision of
information
• People are more likely to seek information if they
believe it will be available and accessible, relevant
and understandable, useful and trustworthy.
• Involving customers in planning how information
and advice are provided, having an organisational
strategy and joining up with other agencies all
help.
• Organisations should use a range of formats,
media and places to provide information (IDEA,
2009).
27
Good practice in the provision of
information
• The third sector, including User Led Organisations
(ULOs), can provide more independent information
and advice (RiPfA, 2011b, 2012b).
• Tailored information and support, often provided
face to face, is particularly important for groups
who face barriers (Putting People First, 2009,
Zahno and Rhule, 2008).
• Centrality of personal relationships: staff need
skills and tools (Newbronner et al, 2011).
• I&A should be followed up on, and information
services reviewed (RiPfA, 2013). 28
Coordinating the provision of
information and advice
29
The TLAP Strategy Tool
30
Takes you
through six
stages of
developing a
local I&A
strategy,
providing
tools,
resources and
case studies.
thinklocalactpersonal.org.uk
An example of good
practice
31
• Maintained by
Healthwatch
• Different
views of the
same data
depending on
your needs
(social care,
mental health,
etc)
How will you meet your information
and advice requirements?
32
Independent Advocacy – why it
matters
33
The letter of the law:
independent advocacy
Section 67 of the Care Act says that a local authority must
provide an independent advocate if an individual would
experience substantial difficulty with one or more of the
following
‘(a) understanding relevant information;
(b) retaining that information;
(c) using or weighing that information as part of the process of
being involved;
(d) communicating the individual’s views, wishes or feelings
(whether by talking, using sign language or any other means).’
34
The duty to provide an independent advocate does
not apply
• if there is ‘an appropriate person to represent and
support the individual’ who is not being paid to
care for them, and as long as
• the individual has given their consent if possible,
or
• if this is not possible, the LA is happy that ‘being
represented and supported by that person would
be in the individual’s best interests’.
35
The letter of the law:
independent advocacy
Advocacy: what does the Guidance
say?
‘The ultimate aim is for people’s wishes, feelings and
needs to be at the heart of the assessment, care
planning and review processes.’
It is the need for people to be involved in decisions
about them that advocacy addresses.
36
• There is a separate requirement for an
independent advocate in the case of a
Safeguarding Adults Review (SAR) (Section 68).
• If an individual already has an advocate, the same
person would ideally play the same role in the
SAR.
• If a safeguarding inquiry needs to start prior to the
appointment of an advocate it can – although the
Guidance notes the particular importance of
advocacy in enabling an adult who may have been
abused or neglected to be involved in the process. 37
Advocacy and safeguarding
A step in the right direction – but
not far enough?
• Consensus that advocacy is of benefit to people
• The Care Act targets advocacy provision by
focusing on issues of communication and
understanding
• This plays down the more fundamental aspect of
ensuring someone’s rights are protected
• Councils can promote and provide advocacy
services more widely than in the narrow
circumstances described in the Act
38
Why would councils provide more
than the statutory minimum?
Better for people
• It protects their rights
• It empowers them (gives them more control)
• Helps them to identify and articulate their outcomes
Better for the organisation
• Wider use of advocacy is efficient at preventing,
delaying and reducing need for care and support.
• It accords with anti-oppressive practice.
39
Advocacy: models and effectiveness
Models of advocacy
• Self-advocacy
• Peer advocacy
• Volunteer citizen
advocacy
• Independent/
professional advocacy
• Non-instructed advocacy
(Stewart and MacIntyre, 2013)
40
iriss.org.uk
A good advocate…
• builds a relationship of trust (Townsley et al, 2009,
Palmer et al, 2012)
• has a clearly defined role and the appropriate
skills, knowledge and experience (Townsley et al,
2009)
• is culturally sensitive
• works either for a service user or a carer
(Stewart and MacIntyre, 2013)
41
Benefits of advocacy
• Promotes people’s rights and supports anti-
oppressive practice
• Greater empowerment, self-efficacy and
confidence
• Greater sense of participation and having one’s
voice heard
42
Evaluating the effectiveness of
advocacy
When considering what works in relation to
advocacy, it is important to separate out the
person’s experience from outcomes
(Featherstone et al, 2012).
This is because not achieving a person’s outcome –
say, that of returning to employment – does not
mean that advocacy didn’t work.
Thanks to the advocate, the person could have been
better represented, more involved in the process and
had a better experience overall.
43
Commissioning independent
advocacy
• Specialist provision is required for groups with
particular support or communication needs
• In such cases, particular training needs must be
addressed
• Advocates need independence from services
(even if funded by them) – but not to be
isolated from them
(Stewart and MacIntyre, 2013) 44
SCIE’s Guide to Commissioning
Independent Advocacy
45
Sections include
• key messages
• advocacy duties
• inclusion
• good practice
• Equality Act
compliance
• scenarios
scie.org.uk
An example of good
practice
46
• Shift from patchwork of 9 different providers
(2007) to a coordinated service (2013)
• Single low cost phone number, staffed by
experienced practitioners
• Quality assured
• People helped increased (over 30%), costs
reduced (by more than 36%)
How will you meet the requirement
to provide independent advocacy?
47
Final thoughts
48
Contact
www.ripfa.org.uk
help@ripfa.org.uk
@ripfa
49

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The Care Act Expert Webinar: Providing good information, advice and advocacy

  • 1. Care Act Expert Webinar Providing Good Information, Advice and Advocacy 1
  • 2. Webinar aims We will explore • The changes to the law regarding information, advice and advocacy and how these fit with the wider aims of the Care Act • The related challenges, and some examples of how these are being addressed in different areas 2
  • 3. Webinar objectives By the end of this webinar, you will have • Begun to consider how effectively your existing services meet the requirements of the Care Act • Identified barriers and enablers to meeting these requirements • Examined key examples of good practice • Started to identify next steps in your area 3
  • 4. Webinar agenda 1. Definitions 2. What’s working at the moment? 3. The changes to the law 4. Getting your own information across 5. Coordinating provision of information and advice 6. Independent advocacy – why it matters 7. Final thoughts 4
  • 6. Definitions from the Care Act Guidance Information means the communication of knowledge and facts regarding care and support. It can be subdivided into ‘self-help’ and ‘assisted’ information Advice means helping a person to identify choices and/or providing an opinion or recommendation regarding a course of action in relation to care and support. 6
  • 7. Definitions from the Care Act Guidance Financial information and advice covers services whose purpose is to help people plan, prepare and pay for their care costs. ‘Independent’ financial information or advice means services independent of the local authority. Advocacy means supporting a person to understand information, express their needs and wishes, secure their rights, represent their interests and obtain the care and support they need. 7
  • 8. A degree of overlap 8 e.g. leaflet; website e.g. helpline, library e.g. social worker, GP e.g. financial advisor e.g. advocate, family member Self-help information Assisted information Advice Specialist advice Advocacy
  • 9. What’s working at the moment? What challenges are you facing in the provision of information, advice and advocacy? In which areas are you well prepared and on track? 9
  • 10. Changes to the law 10
  • 11. The wider context of the Care Act • Long overdue bringing together of the patchwork of adult social care legislation • Changing relationship between people and services • A move from dependency to empowerment – assisting people and communities to find sustainable solutions • Dwindling resources and increased demand 11
  • 12. Empowerment Two senses: 1. Giving power (whether political, social or economic) to someone • This is what underlies notions of co-production Or 2. Supporting someone to claim personal power. • This is what underlies person-centred care and an outcomes-based approach. 12
  • 13. How does the Care Act empower? 1. Universal access to information and advice 1. Informing people so they can make the best choices for themselves: starting from the notion that people are experts in what’s best for them 2. This responsibility extends to all citizens, not just those with eligible needs 3. This links to the council’s preventative role: it empowers people by helping to keep their options open; by preventing/delaying/reducing needs for care and support. 13
  • 14. How does the Care Act empower? 2. Improved access to advocacy 1. Although far from universal (as we’ll see below), the role of independent advocacy is a recognition of the power of advocacy 2. LAs have the option of providing advocacy more widely than the Care Act requires. Rather than simply a communication aid, advocacy can be seen as protector of the person’s human rights. 14
  • 15. The prevention agenda The provision of information, advice and advocacy is part of addressing the aim of preventing, delaying and reducing people’s need for care and support: • With good information and advice, people can make better, healthier decisions • It is important for tackling the issue of multiple needs and exclusions • help to access specialist support or common interest groups • advocacy promotes the individual’s rights and interests and hence their wellbeing 15
  • 16. The letter of the law: information and advice Section 4 of the Care Act specifies that an LA must ‘establish and maintain a service for providing people in its area with information and advice relating to care and support for adults and support for carers’ including • Types of care and support available and how to access it • How to access independent financial advice • How to raise concerns 16
  • 17. The letter of the law: information and advice The LA must also • ensure information and advice provided is accessible and proportionate • ‘have regard to the importance of identifying those individuals’ who would benefit from financial advice • Make sure that this advice is good enough to allow them to plan and make decisions about their own care. 17
  • 18. Information and advice: what does the Guidance say? It is the LA’s responsibility to ensure the • COHERENCE • SUFFICIENCY • AVAILABILITY • ACCESSIBILITY of information and advice relating to care and support across its area (p23) 18
  • 19. As well as covering basic information about what care and support is available, this service needs to cover • prevention of care and support needs • finances • health • housing • employment • what to do in cases of abuse or neglect of an adult and other areas where required (p23-24) 19 Information and advice: what does the Guidance say?
  • 20. This duty is about • engaging with and understanding the needs of people in your area and • ensuring that the requirement to provide information is met in the most appropriate way – whether by the authority or another organisation. • It falls on the authority to ‘understand, co-ordinate and make effective use of’ other I&A resources in your area 20 Information and advice: what does the Guidance say?
  • 21. The particular needs of carers may include: • breaks from caring; • the health and wellbeing of carers themselves; • caring and advice on wider family relationships; • carers’ financial and legal issues; • caring and employment; • caring and education; and, • a carer’s need for advocacy. 21 Information and advice: what does the Guidance say?
  • 22. Getting your own information across 22
  • 23. Skills for Care resources 23 skillsforcare.org.uk Provides slide packs, summaries, a workbook and case studies. Can be used as the basis for staff development.
  • 24. The RiPfA Practice Tool 24 ripfa.org.uk • Outlines good practice regarding information provision for different groups • Helps you audit the information you provide • Helps you ask service users and carers what is working and not working • Tool to support reflection
  • 25. Challenges in the provision of information • Generally people do not have a good understanding of adult social care and there may be stigma in approaching it (ADASS, 2011). • Often people first seek information at a time of crisis (Bottery and Holloway, 2013). • Uncoordinated services will result in uncoordinated, unreliable information (Anderson, 2011) 25
  • 26. Challenges in the provision of information • Older people are less likely to use the internet or call centres (Horton, 2009) • BME groups face cultural and linguistic barriers (Zahno and Rhule, 2008). An equality impact assessment on the provision of information can address this (c.f. Newham’s safeguarding work – see RiPfA blog 13/3/14) • Self-funders may not be seen as a priority (Hudson and Henwood, 2009) • Many people face difficulties with communication or capacity (IDEA, 2009) • People who face stigma are less likely to engage with social care (RiPfA, 2013). 26
  • 27. Good practice in the provision of information • People are more likely to seek information if they believe it will be available and accessible, relevant and understandable, useful and trustworthy. • Involving customers in planning how information and advice are provided, having an organisational strategy and joining up with other agencies all help. • Organisations should use a range of formats, media and places to provide information (IDEA, 2009). 27
  • 28. Good practice in the provision of information • The third sector, including User Led Organisations (ULOs), can provide more independent information and advice (RiPfA, 2011b, 2012b). • Tailored information and support, often provided face to face, is particularly important for groups who face barriers (Putting People First, 2009, Zahno and Rhule, 2008). • Centrality of personal relationships: staff need skills and tools (Newbronner et al, 2011). • I&A should be followed up on, and information services reviewed (RiPfA, 2013). 28
  • 29. Coordinating the provision of information and advice 29
  • 30. The TLAP Strategy Tool 30 Takes you through six stages of developing a local I&A strategy, providing tools, resources and case studies. thinklocalactpersonal.org.uk
  • 31. An example of good practice 31 • Maintained by Healthwatch • Different views of the same data depending on your needs (social care, mental health, etc)
  • 32. How will you meet your information and advice requirements? 32
  • 33. Independent Advocacy – why it matters 33
  • 34. The letter of the law: independent advocacy Section 67 of the Care Act says that a local authority must provide an independent advocate if an individual would experience substantial difficulty with one or more of the following ‘(a) understanding relevant information; (b) retaining that information; (c) using or weighing that information as part of the process of being involved; (d) communicating the individual’s views, wishes or feelings (whether by talking, using sign language or any other means).’ 34
  • 35. The duty to provide an independent advocate does not apply • if there is ‘an appropriate person to represent and support the individual’ who is not being paid to care for them, and as long as • the individual has given their consent if possible, or • if this is not possible, the LA is happy that ‘being represented and supported by that person would be in the individual’s best interests’. 35 The letter of the law: independent advocacy
  • 36. Advocacy: what does the Guidance say? ‘The ultimate aim is for people’s wishes, feelings and needs to be at the heart of the assessment, care planning and review processes.’ It is the need for people to be involved in decisions about them that advocacy addresses. 36
  • 37. • There is a separate requirement for an independent advocate in the case of a Safeguarding Adults Review (SAR) (Section 68). • If an individual already has an advocate, the same person would ideally play the same role in the SAR. • If a safeguarding inquiry needs to start prior to the appointment of an advocate it can – although the Guidance notes the particular importance of advocacy in enabling an adult who may have been abused or neglected to be involved in the process. 37 Advocacy and safeguarding
  • 38. A step in the right direction – but not far enough? • Consensus that advocacy is of benefit to people • The Care Act targets advocacy provision by focusing on issues of communication and understanding • This plays down the more fundamental aspect of ensuring someone’s rights are protected • Councils can promote and provide advocacy services more widely than in the narrow circumstances described in the Act 38
  • 39. Why would councils provide more than the statutory minimum? Better for people • It protects their rights • It empowers them (gives them more control) • Helps them to identify and articulate their outcomes Better for the organisation • Wider use of advocacy is efficient at preventing, delaying and reducing need for care and support. • It accords with anti-oppressive practice. 39
  • 40. Advocacy: models and effectiveness Models of advocacy • Self-advocacy • Peer advocacy • Volunteer citizen advocacy • Independent/ professional advocacy • Non-instructed advocacy (Stewart and MacIntyre, 2013) 40 iriss.org.uk
  • 41. A good advocate… • builds a relationship of trust (Townsley et al, 2009, Palmer et al, 2012) • has a clearly defined role and the appropriate skills, knowledge and experience (Townsley et al, 2009) • is culturally sensitive • works either for a service user or a carer (Stewart and MacIntyre, 2013) 41
  • 42. Benefits of advocacy • Promotes people’s rights and supports anti- oppressive practice • Greater empowerment, self-efficacy and confidence • Greater sense of participation and having one’s voice heard 42
  • 43. Evaluating the effectiveness of advocacy When considering what works in relation to advocacy, it is important to separate out the person’s experience from outcomes (Featherstone et al, 2012). This is because not achieving a person’s outcome – say, that of returning to employment – does not mean that advocacy didn’t work. Thanks to the advocate, the person could have been better represented, more involved in the process and had a better experience overall. 43
  • 44. Commissioning independent advocacy • Specialist provision is required for groups with particular support or communication needs • In such cases, particular training needs must be addressed • Advocates need independence from services (even if funded by them) – but not to be isolated from them (Stewart and MacIntyre, 2013) 44
  • 45. SCIE’s Guide to Commissioning Independent Advocacy 45 Sections include • key messages • advocacy duties • inclusion • good practice • Equality Act compliance • scenarios scie.org.uk
  • 46. An example of good practice 46 • Shift from patchwork of 9 different providers (2007) to a coordinated service (2013) • Single low cost phone number, staffed by experienced practitioners • Quality assured • People helped increased (over 30%), costs reduced (by more than 36%)
  • 47. How will you meet the requirement to provide independent advocacy? 47

Editor's Notes

  1. As we’ll see, the Care Act makes it the LA’s duty to provide these to all citizens, not just those with eligible needs.
  2. As we’ll see, advocacy differs in that its provision is targeted rather than universal.
  3. (Adapted from Skills for Care 2014 (which lumps specialist advice together with advocacy – however, these are better separated because the latter is more likely to be a longer term relationship; the relationship can be an end in itself.) It can be difficult to unpick information, advice and advocacy services, since for many users of care and support, these three types of service provision overlap and are inter-related. In order to access the right services and/or information, people may require support from each of these types of services, and they do not always follow a linear progression (such as the person moving from a position of requiring information to advice and then advocacy). It may be helpful therefore to think of it as a spectrum of information and advice ‘activity’ with overlaps between the groupings. Four types of activity are identified in this spectrum – self-help information, assisted information, advice, and specialist advice and advocacy - along with examples of common delivery mechanisms for these activities and their likely associated level of interaction between the person needing information and advice and those providing it.
  4. Feedback from participants and/or discussion based on surveymonkey responses
  5. 1. …much of the existing legislation very dated with attitudes/terminology to match. Rather than fitting the person to the existing service, the relationship is much more individualised and focused on promoting the individual’s wellbeing and outcomes, encouraging them to look to their communities for support. From the organisational point of view, this is about doing more with less. Councils having to make further savings; ageing population + other Care Act responsibilities including assessing and keeping track of self funders and the new prominence of carers’ assessments.
  6. Both these definitions relate to the underlying principle of the Care Act, of putting people in control of their own care, i.e. they, to a greater extent, say what they want to happen to them and what they want their care to achieve. NB: there is some debate about the extent of the control granted by the Care Act. See for example Beresford, who points out that, despite the wording of the Care Act, the final decision about what’s right for a person remain with the local authority. NB: a second caveat is to do with the backdrop of shrinking resources. A question we will return to is whether the focus on IAA is merely cover for a withdrawal of services, with people being expected to fend for themselves. We will argue, that if done properly, the provision of IA&A is part of a new relationship of better partnership working with communities and responding to needs in a more effective, sustainable way.
  7. definitions of information and advice provided above
  8. Definition of advocacy provided above
  9. Multiple needs and exclusions: The lack of targeted information at points of transition – such as the point of release from prison – is seen by service users as a ‘major weakness in the system’ and can feed into or perpetuate the situation of those with multiple needs and exclusions (MNE Lit Review, RiPfA 2014, citing Braithwaite et al, 2009)
  10. -Financial advice about care and support -Concerns about the safety of an adult with care and support needs.
  11. Opportunity to raise questions about any of these four terms
  12. …these other resources may be from the statutory, voluntary or private sector.
  13. p27 of the Guidance
  14. This slide to be replaced/followed by Fiona’s presentation.
  15. Barriers facing specific groups. NB it wouldn’t just be older people who might be excluded by internet-only information provision, but anyone without access to the technology – especially in the face of library closures. Two prongs in response are low cost, refurbished computer schemes + free beginners’ IT classes – funding for these can be drawn down from the Skills Funding Agency The availability of face-to-face or telephone information and advice Issues to do with the decimation of translation services Blog on Newham: https://www.ripfa.org.uk/blog/entry/newham-engaging-the-asian-community-in-safeguarding
  16. Aimed at those such as council officers who are developing a local I&A strategy.
  17. Participant feedback How has the above influenced your thinking? What steps are needed in your area? How will you ensure the quality of the information that’s available? What additional support do you need?
  18. Independent = independent of the authority
  19. “in the personalisation approach”. [said Carl Evans, architect of the advocacy section of the Act, National Advocacy Conference (Oct 14), ] “it was clear from the start that everyone regards advocacy as a good thing” (Peter Beresford, The Guardian 2/12/14 http://www.theguardian.com/social-care-network/2014/dec/02/care-act-2015-service-users-power-social Why would councils provide more than the statutory minimum? To protect people’s rights To improve their outcomes To prevent, delay and reduce their need for care and support To empower people in any case where their interests are at risk.
  20. More efficient: An advocate helps you establish what a person actually needs and wants, helping you avoid wasting resources getting it wrong.
  21. Self-advocacy promotes confidence, skills and knowledge and protection of individual rights (Lawton, 2009). Peer advocacy hinges on shared experience/membership of the same group Volunteer (unpaid) advocacy is like a deeper version of befriending, where the relationship is an end in itself Independent/professional (paid) advocacy – by being independent of the LA, this answers the challenge of practitioners’ dilemma of advocating on behalf of a person while at the same time managing scarce resources. The independent advocate can even help to bridge damaged relations between the person and social worker. Non-instructed: where the person’s capacity to instruct is impaired. The non-instructed advocate works for the person’s rights and to promote their wellbeing and uses every means available to communicate with them.
  22. relationship of trust built on continuity, consistency and familiarity. This has implications for advocacy on a short-term or one-off basis. having the appropriate skills, knowledge and experience entails training and ongoing support. Cultural sensitivity = understanding of the issues facing particular groups separating needs of service users and carers is essential to ensure conflicts do not arise.
  23. Adapted from IRISS (2013)
  24. See our previous Care Act webinar for Patrick Hall of SCIE talking about the guide for commissioning. LAs need to establish flexible mechanisms to begin with – perhaps think about how existing services can meet new demand.
  25. This slide to be replaced or followed by Shalini’s presentation.
  26. Participant feedback How has the above influenced your thinking? What next steps are needed in your area? How will you ensure the quality of advocacy provision? What additional support do you need?
  27. Conclusions – summing up points people have made and positive steps to take. Forthcoming events/resources References from today will be circulated and this presentation will be available to view on our website soon.